Duns Number:306032491
Device Description: Single use infusion set for subcutaneous infusion. The infusion set must be used as descri Single use infusion set for subcutaneous infusion. The infusion set must be used as described in the Instruction for Use.
Catalog Number
-
Brand Name
Mio Advance
Version/Model Number
MMT-243AT
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K173879,K173879,K173879
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
cf336962-2795-4ced-a0a9-621597e9c274
Public Version Date
February 11, 2021
Public Version Number
1
DI Record Publish Date
February 03, 2021
Package DI Number
05705244025189
Quantity per Package
36
Contains DI Package
05705244025172
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Outer box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 14 |